Responsible for compliance of the Validation Master Plan of the Plant, and in charge of follow up of execution of all tasks included in it. Reviewer of Installation, Operational and Performance Qualification Protocols and Reports and Test Methods Validation as well. Key contact of Validation Department in topics related to Process Transfer. SME of Validation Process for MDSAP Audits. Lead of Validations for Transfer Process from USA to Costa Rica of Medical Devices Class II. Management of Non-Conformities, CAPAs, SCARs, Change Controls, Document Controls and responsible to ensure compliance with Good Documentation Practices in Validation Documents.

Responsible for compliance with Good Manufacturing Practices and Good Laboratory Practices in the Physicochemical, Microbiological and Incoming areas. Responsible for the supervision and coordination of analyses carried out in laboratory areas, with 11 direct reports for the execution the tasks assigned to the Quality Control Laboratory. Responsible for coordinating and negotiating with the Logistics Department the dates of entry of materials, as well as the approval of these and the finished products. Responsible for compliance with 100% of all safety, health and environmental (EHS) guidelines. Reviewer of all the Validation Protocols and Reports related with Analytical Equipment. In charge of all the Documentation System of the Laboratory (SOP´s, Policies) and all the Quality Systems needed for the operation of the area (OOS, Data Integrity, CAPA, RCA). Responsible for compliance off all the support systems required for the operation of the laboratory (reagents, equipment calibration) and the follow up of all the KPI´s of the Quality Control Area.

Responsible for ensuring that all Quality Systems of the plant are kept in control and validated, in addition to ensuring that the company's products meet the quality standards established by regulatory entities and the corporation and that they meet the needs of customers. Responsible for the maintenance of The Quality Culture at the Site Responsible for safely and effectively coordinating quality operations. Planning and ensuring compliance with the department's budget. I lead 15 direct reports and 7 indirect reports to perform all tasks related to the Areas of the Quality Department. Responsible for all official communications related to Quality events to the Site and to the regional and global levels of the organization.

- Docente Curso Análisis de Medicamentos II- Docente Curso Análisis de Medicamentos III

responsible for all technical aspects (formulation, performance) related to liquid and semi-solid products of the San José Plant. Responsible for the sustaining operations of the plant (maintenance of the validated status of all processes of the San José plant for both Liquids, Semi-solids and Effervescent Powders products). Responsible for the Life Cycle Management of Plant Products (performance of the processes and Quality Control Results, Cpk, Ppk, etc) and Process Transference of Products. Work with 1 direct report (Process Engineer).

Responsible for the execution of the tasks included in the Site Validation Master Plan of the Plant as well as the programming of spaces for the execution of the Cleaning and Process Validations with the Logistics area, in addition to the training of the operational and administrative personnel of the plant in topics related to Process Validations and in general with the Life Cycle of Process and Product Validation.

• Manejo de patentes comerciales, presentaciones y dosis.• Consulta y Recomendación Farmacéutica• Despacho de Recetas• Manejo y Despacho de Psicotrópicos y Estupefacientes• Aplicación de Inyectables• Toma de Presión Arterial• Atención al Cliente

• Manejo de patentes comerciales, presentaciones y dosis.• Consulta y Recomendación Farmacéutica• Despacho de Recetas• Manejo y Despacho de Psicotrópicos y Estupefacientes• Aplicación de Inyectables• Toma de Presión Arterial• Atención al Cliente

Responsible for the establishment and execution of activities of the Plant Cleaning Validation Program in addition to the Environmental Conditions Mapping Tasks in the main Warehouses of the Production Plant, as well as the start of the Validation of the Purified Water System.

• Resolución de consultas vía Telefónica acerca de los productos de la compañía.• Oferta de Campañas de Vacunación y Desparasitación Vía Telefónica.• Farmacovigilancia.